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Measuring the dose in bone for spine stereotactic body radiotherapy
Affiliation:1. Australian Clinical Dosimetry Service, Australian Radiation Protection and Nuclear Safety Agency, Melbourne, Australia;2. School of Health and Biomedical Sciences, RMIT University, Melbourne, Australia;3. Olivia Newton John Cancer Wellness Centre, Melbourne, Australia;4. Primary Standards Dosimetry Laboratory, ARPANSA, Melbourne, Australia;5. Department of Radiation Oncology, Calvary Mater Newcastle, Newcastle, Australia;6. School of Science, RMIT University, Melbourne, Australia;7. School of Mathematical and Physical Sciences, University of Newcastle, Australia;8. Institute of Medical Physics, University of Sydney, Australia;9. Alfred Health Radiation Oncology, The Alfred Hospital, Melbourne, Australia;10. Australian Radiation Protection and Nuclear Safety Agency, Melbourne, Australia
Abstract:PurposeCurrent quality assurance of radiotherapy involving bony regions generally utilises homogeneous phantoms and dose calculations, ignoring the challenges of heterogeneities with dosimetry problems likely occurring around bone. Anthropomorphic phantoms with synthetic bony materials enable realistic end-to-end testing in clinical scenarios. This work reports on measurements and calculated corrections required to directly report dose in bony materials in the context of comprehensive end-to-end dosimetry audit measurements (63 plans, 6 planning systems).Materials and methodsRadiochromic film and microDiamond measurements were performed in an anthropomorphic spine phantom containing bone equivalent materials. Medium dependent correction factors, kmed, were established using 6 MV and 10 MV Linear Accelerator Monte Carlo simulations to account for the detectors being calibrated in water, but measuring in regions of bony material. Both cortical and trabecular bony material were investigated for verification of dose calculations in dose-to-medium (Dm,m) and dose-to-water (Dw,w) scenarios.ResultsFor Dm,m calculations, modelled correction factors for cortical and trabecular bone in film measurements, and for trabecular bone in microDiamond measurements were 0.875(±0.1%), 0.953(±0.3%) and 0.962(±0.4%), respectively. For Dw,w calculations, the corrections were 0.920(±0.1%), 0.982(±0.3%) and 0.993(±0.4%), respectively. In the audit, application of the correction factors improves the mean agreement between treatment plans and measured microDiamond dose from −2.4%(±3.9%) to 0.4%(±3.7%).ConclusionMonte Carlo simulations provide a method for correcting the dose measured in bony materials allowing more accurate comparison with treatment planning system doses. In verification measurements, algorithm specific correction factors should be applied to account for variations in bony material for calculations based on Dm,m and Dw,w.
Keywords:SBRT  Dosimetry audit  Dosimetry  Quality assurance  Dose to medium
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